Canonical Allele Identifier: PA275665
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 204089
ClinVar RCV Id: RCV000186295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000021.1:p.Trp108Cys
CA275664
NM_000030.3:c.324G>T
CA351313855
NM_000030.3:c.324G>C